Phenotypes associated with this allele

• Allele Symbol: Fam20a^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548797
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Fam20a^tm1b(KOMP)Wtsi/Fam20a^tm1b(KOMP)Wtsi	C57BL/6N-Fam20a^tm1b(KOMP)Wtsi/Ucd	MGI:5631115

Genotype
MGI:5631115

hm1

• Allelic Composition: Fam20a^{tm1b(KOMP)Wtsi}/Fam20a^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Fam20a^{tm1b(KOMP)Wtsi}/Ucd
• Cell Lines: EPD0267_2_B02

Data Sources

IMPC Data for Fam20a

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

adipose tissue

decreased total body fat amount ( J:211773 )

♀

IMPC - UCD

craniofacial

abnormal tooth morphology ( J:211773 )

♀

IMPC - UCD

growth/size/body

abnormal tooth morphology ( J:211773 )

♀

IMPC - UCD

limbs/digits/tail

short tibia ( J:211773 )

IMPC - UCD

renal/urinary system

abnormal kidney morphology ( J:211773 )

♀

IMPC - UCD

skeleton

abnormal tooth morphology ( J:211773 )

♀

IMPC - UCD

short tibia ( J:211773 )

IMPC - UCD

increased bone mineral content ( J:211773 )

♀

IMPC - UCD

vision/eye

cornea opacity ( J:211773 )

IMPC - UCD